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The meeting showcased rare skin disease cases, highlighting the need for accurate diagnosis and treatment.

The woman's rare combination of diseases suggests an unknown factor may predispose individuals to multiple endocrine diseases.

A patient with a rare chromosome condition also had a rare type of hair loss.

A boy with a rare birthmark called verrucous hemangioma needed careful timing for surgery due to its size and depth.

Syphilitic alopecia is a rare hair loss condition in secondary syphilis that looks similar to another condition but can be diagnosed with specific tests and responds to antibiotics.

Lichen planopilaris is a rare, chronic condition causing hair loss, mainly in middle-aged women, and early treatment is important to prevent permanent baldness.

A man had a rare skin reaction from a hair loss medication, which improved after stopping the drug.

Two siblings have a rare genetic condition causing curly, coarse hair.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Two patients had a rare combination of red skin spots and white scaly skin lesions not on the genitals.

RAPK is a rare skin disorder with pigmented spots, mainly on hands and feet, starting in youth.

Finasteride can cause rare but serious skin rashes.

Post-finasteride syndrome is rarely linked to sexual and systemic side effects.

Finasteride might cause rare blood clot in brain for baldness patients.

New insights show Lichen Planopilaris is a rare, scarring hair loss condition, hard to treat, mainly affecting middle-aged women, and significantly impacts mental health.

Allergic reactions to blood thinners are rare but can be serious, requiring careful testing and alternative treatments.

Male accessory sex glands in rats rarely develop tumors and respond to hormones.

Pityriasis rubra pilaris is a rare skin disorder with reddish-orange patches and thickened skin, needing better treatment understanding.

Skin problems in COVID-19 patients are rare and may be due to the body's complex immune response or blood clotting issues.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A 93-year-old woman developed a rare scalp condition after therapy, which improved with steroids, not antibiotics.

A woman with breast cancer developed a rare condition causing excessive fine hair growth on her face and body.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Erosive pustular dermatosis is a rare skin disease that's hard to treat and affects the scalp or legs.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

Congenital alopecia in domestic animals is rare and involves abnormal hair follicle development, needing better understanding and classification.

SACUMAN, a rare condition causing hair loss without clear signs, is often misdiagnosed and needs scalp biopsies for accurate detection.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Some stem cells in the body rarely divide, which could help create better treatments for diseases and aging.